Understanding α-Globin Gene Regulation: Aiming to Improve the Management of Thalassemia von HIGGS, D.R., GARRICK, D., ANGUITA, E., DE GOBBI, M., HUGHES, J., MUERS, M., VERNIMMEN, D., LOWER, K., LAW, M., ARGENTARO, A., DEVILLE, M. A., GIBBONS, R.

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The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22 von Camaschella, Clara, Roetto, Antonella, Calì, Angelita, De Gobbi, Marco, Garozzo, Giovanni, Carella, Massimo, Majorano, Nunzia, Totaro, Angela, Gasparini, Paolo

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Annotation of Cis-Regulatory Elements by Identification, Subclassification, and Functional Assessment of Multispecies Conserved Sequences von Hughes, Jim R., Cheng, Jan-Fang, Ventress, Nicki, Prabhakar, Shyam, Clark, Kevin, Anguita, Eduardo, De Gobbi, Marco, de Jong, Pieter, Rubin, Eddy, Higgs, Douglas R., Weatherall, David

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New mutations inactivating transferrin receptor 2 in hemochromatosis type 3 von Roetto, Antonella, Totaro, Angela, Piperno, Alberto, Piga, Antonio, Longo, Filomena, Garozzo, Giovanni, Calı̀, Angelita, De Gobbi, Marco, Gasparini, Paolo, Camaschella, Clara

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Juvenile hemochromatosis associated with β-thalassemia treated by phlebotomy and recombinant human erythropoietin von DE GOBBI, Marco, PASQUERO, Paolo, BRUNELLO, Franco, PACCOTTI, Piero, MAZZA, Umberto, CAMASCHELLA, Clara

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Natural history of juvenile haemochromatosis von De Gobbi, Marco, Roetto, Antonella, Piperno, Alberto, Mariani, Raffaella, Alberti, Federica, Papanikolaou, George, Politou, Marianna, Lockitch, Gillian, Girelli, Domenico, Fargion, Silvia, Cox, Thimoty M., Gasparini, Paolo, Cazzola, Mario, Camaschella, Clara

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Diagnosis of juvenile hemochromatosis in an 11-year-old child combining genetic analysis and non-invasive liver iron quantitation von DE GOBBI, M, CARUSO, R, DARAIO, F, CHIANALE, F, PINTO, R. M, LONGO, F, PIGA, A, CAMASCHELLA, C

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Juvenile hemochromatosis von Camaschella, Clara, Roetto, Antonella, De Gobbi, Marco

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Busulfan or Treosulfan Conditioning Platform for Allogeneic Stem Cell Transplantation in Patients Aged >60 Y With Acute Myeloid Leukemia/Myelodysplastic Syndrome: A Subanalysis of... von Malagola, Michele, Polverelli, Nicola, Martino, Massimo, Patriarca, Francesca, Bruno, Benedetto, Giaccone, Luisa, Grillo, Giovanni, Bramanti, Stefania, Bernasconi, Paolo, De Gobbi, Marco, Natale, Annalisa, Terruzzi, Elisabetta, Olivieri, Attilio, Chiusolo, Patrizia, Carella, Angelo Michele, Casini, Marco, Maffini, Enrico, Nozzoli, Chiara, Mazza, Patrizio, Bassi, Simona, Onida, Francesco, Vacca, Adriana, Falcioni, Sadia, Luppi, Mario, Iori, Anna Paola, Pavone, Vincenzo, Skert, Cristina, Carluccio, Paola, Borghero, Carlo, Proia, Anna, Selleri, Carmine, Rubini, Vicky, Sacchi, Nicoletta, Oldani, Elena, Bonifazi, Francesca, Ciceri, Fabio, Russo, Domenico

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Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations von Bosio, Sandra, De Gobbi, Marco, Roetto, Antonella, Zecchina, Gabriella, Leonardo, Eugenio, Rizzetto, Mario, Lucetti, Claudio, Petrozzi, Lucia, Bonuccelli, Ubaldo, Camaschella, Clara

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Genetic haemochromatosis: genes and mutations associated with iron loading von Camaschella, Clara, Roetto, Antonella, De Gobbi, Marco

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Hemochromatosis Due to Mutations in Transferrin Receptor 2 von Roetto, Antonella, Daraio, Filomena, Alberti, Federica, Porporato, Paolo, Calı̀, Angelita, De Gobbi, Marco, Camaschella, Clara

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Interplay between DNA and histone methylation at an α-globin gene silenced by antisense RNA von De Gobbi, M., Sloane Stanley, J.A., Ayyub, H., Wood, G.W., Higgs, D.R., Tufarelli, C.

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Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience von De Gobbi, M, D'Antico, S, Castagno, F, Testa, D, Merlini, R, Bondi, A, Camaschella, C

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Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload von De Gobbi, M, Daraio, F, Oberkanins, C, Moritz, A, Kury, F, Fiorelli, G, Camaschella, C

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HETEROZYGOUS β- THALASSEMIA AND HOMOZYGOUS H63D HEMOCHROMATOSIS IN A CHILD: An 18-Year Follow-Up von Miniero, Roberto, Tardivo, Irene, Roetto, Antonella, Gobbi, Marco De

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TFR2 Y250X mutation in Italy von De Gobbi, M, Barilaro, M R, Garozzo, G, Sbaiz, L, Alberti, F, Camaschella, C

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DIAGNOSIS AND MANAGEMENT OF HAEMOCHROMATOSIS SINCE THE DISCOVERY OF THE HFE GENE: A EUROPEAN EXPERIENCE von Robson, K J H, Merryweather, A T, Pointon, J J, Shearman, J D

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Mutual Guarantee Associations for Small and Micro-Entrepreneurs: Lessons Learned from Europe and Africa von De Gobbi, Maria Sabrina

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Juvenile hemochromatosis associated with B-thalassemia treated by phlebotomy and recombinant human erythropoietin von De Gobbi, M, Pasquero, P, Brunello, F, Paccotti, P, Mazza, U, Camaschella, C

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